- Conditions
- Artemis (DCLRE1C ) Deficient Severe Combined Immunodeficiency, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, +10 more
- Locations
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- Department of Pediatric Immunology, Hematology and Rheumatology UIHR, Necker-Enfants Malades Hospital Paris, France
Clinical trial condition
Xeroderma Pigmentosum, Complementation Group F
Explore clinical trials studying Xeroderma Pigmentosum, Complementation Group F. Study availability and eligibility vary by location and protocol.
1 public trial
1 recruiting study
Xeroderma Pigmentosum, Complementation Group F trial results
Related conditions
- Artemis (DCLRE1C ) Deficient Severe Combined Immunodeficiency (1)
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)
- DNA Repair-Deficiency Disorders (1)
- Genetic Diseases, Inborn (1)
- Immune System Diseases (1)
- Immunologic Deficiency Syndromes (1)
- Infant, Newborn, Diseases (1)
- Metabolic Diseases (1)